1433-27-8 Usage
Uses
Used in Chemical Synthesis:
1-TERT-BUTYL-3-ETHYLCARBODIIMIDE is used as a reactant for the guanylation of amines, which is a crucial step in the synthesis of various organic compounds and pharmaceuticals.
Used in Materials Science:
1-TERT-BUTYL-3-ETHYLCARBODIIMIDE is used as a precursor in the synthesis of tantalum dimethylamido diamidato and guanidinato complexes. These complexes are essential for the chemical vapor deposition (CVD) of nitride thin films, which are utilized in the semiconductor industry for creating electronic devices.
Used in Electronics:
1-TERT-BUTYL-3-ETHYLCARBODIIMIDE is used as a precursor for the preparation of titanium amidinate guanidinate alkylamide complex precursors. These precursors are vital in the formation of HfO2 films, which are widely used as insulating layers in the microelectronics industry.
Used in Pharmaceutical Research:
1-TERT-BUTYL-3-ETHYLCARBODIIMIDE is used in ketene cycloadditions and hydroamination of carbodiimides using group-2-element amides as precatalysts. These reactions are essential for the development of new pharmaceutical compounds and the study of their properties.
Used in Coordination Chemistry:
1-TERT-BUTYL-3-ETHYLCARBODIIMIDE is used in the synthesis of cobalt amidinato derivative complexes. These complexes are crucial for studies involving thermal stability, vapor pressure, vaporization rate, and thermal decomposition properties, which are essential for understanding the behavior of materials under various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1433-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1433-27:
(6*1)+(5*4)+(4*3)+(3*3)+(2*2)+(1*7)=58
58 % 10 = 8
So 1433-27-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2/c1-5-8-6-9-7(2,3)4/h5H2,1-4H3
1433-27-8Relevant academic research and scientific papers
Synthesis of N,N′-carbonyl-bis-amino acids and N,N′-carbonyl-bis-peptides
Izdebski,Pawlak
, p. 1066 - 1074 (2007/10/03)
A new method for the preparation of N,N′-carbonyl-bis-amino acid esters by reaction of bis(4-nitrophenyl)carbonate with amino acid esters is described. When the carbonate reacts with two equivalents of a peptide ester, N,N′-carbonyl-bis(peptide ester) is obtained but, a hydantoin derivative is formed as a side product. The hydantoin derivative is a major product, when equimolar amounts are allowed to react. Usefulness of this method for preparation of larger N,N′carbonyl-bis-peptides is demonstrated by the synthesis of the respective product from C-terminal hexapeptide of Substance P linked to the Merrifield resin.
1-(Triphenylphosphorylideneaminomethyl)benzotriazole (BETMIP) a Novel +CH2N= Synthetic Equivalent: Its Application to the Synthesis of Carbodiimides, Imines, Isothiocyanates, Aziridines, and Secondary Amines
Katritzky, Alan R.,Jiang, Jinglong,Urogdi, Laszlo
, p. 565 - 567 (2007/10/02)
One-carbon homologation has been achieved in novel syntheses of the title compounds by one-pot reaction of 1-(triphenylphosphorylideneaminomethyl)benzotriazole (1) with Grignard reagents followed by in situ transformations of the phosphorazene functionality with isocyanates, aldehydes, carbon disulfide, ethylene oxide, and alkyl halides, respectively.
